CA3043162A1 - Procede et installation pour produire une polyolefine - Google Patents
Procede et installation pour produire une polyolefine Download PDFInfo
- Publication number
- CA3043162A1 CA3043162A1 CA3043162A CA3043162A CA3043162A1 CA 3043162 A1 CA3043162 A1 CA 3043162A1 CA 3043162 A CA3043162 A CA 3043162A CA 3043162 A CA3043162 A CA 3043162A CA 3043162 A1 CA3043162 A1 CA 3043162A1
- Authority
- CA
- Canada
- Prior art keywords
- water
- input stream
- catalyst
- reaction
- reaction input
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 86
- 230000008569 process Effects 0.000 title claims abstract description 81
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 24
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims abstract description 20
- 238000006243 chemical reaction Methods 0.000 claims abstract description 121
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 97
- 229910001868 water Inorganic materials 0.000 claims abstract description 92
- 239000003054 catalyst Substances 0.000 claims abstract description 70
- 238000005839 oxidative dehydrogenation reaction Methods 0.000 claims abstract description 41
- 239000007789 gas Substances 0.000 claims abstract description 40
- 230000000694 effects Effects 0.000 claims abstract description 38
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 30
- 239000001301 oxygen Substances 0.000 claims abstract description 30
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 30
- 239000012188 paraffin wax Substances 0.000 claims abstract description 20
- 230000002829 reductive effect Effects 0.000 claims description 33
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 31
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 24
- 239000003085 diluting agent Substances 0.000 claims description 17
- 239000001569 carbon dioxide Substances 0.000 claims description 12
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 239000002826 coolant Substances 0.000 claims description 10
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 239000011261 inert gas Substances 0.000 claims description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims description 2
- 239000010955 niobium Substances 0.000 claims description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 2
- 229910052714 tellurium Inorganic materials 0.000 claims description 2
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 67
- 239000000463 material Substances 0.000 description 39
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 24
- 239000005977 Ethylene Substances 0.000 description 24
- 229960000583 acetic acid Drugs 0.000 description 22
- 239000000203 mixture Substances 0.000 description 18
- 238000001816 cooling Methods 0.000 description 12
- 238000000926 separation method Methods 0.000 description 10
- 239000006227 byproduct Substances 0.000 description 9
- 229930195733 hydrocarbon Natural products 0.000 description 9
- 150000002430 hydrocarbons Chemical class 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 230000001603 reducing effect Effects 0.000 description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 229910002091 carbon monoxide Inorganic materials 0.000 description 7
- 230000008859 change Effects 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- 238000010791 quenching Methods 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 230000036961 partial effect Effects 0.000 description 5
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000006978 adaptation Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001728 carbonyl compounds Chemical class 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052756 noble gas Inorganic materials 0.000 description 2
- 150000002835 noble gases Chemical class 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000004230 steam cracking Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000012455 biphasic mixture Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000010327 methods by industry Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/42—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor
- C07C5/48—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor with oxygen as an acceptor
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/02—Alkenes
- C07C11/04—Ethylene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/20—Vanadium, niobium or tantalum
- C07C2523/22—Vanadium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/24—Chromium, molybdenum or tungsten
- C07C2523/28—Molybdenum
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
- C07C2523/56—Platinum group metals
- C07C2523/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tatalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/648—Vanadium, niobium or tantalum
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
- C07C2523/56—Platinum group metals
- C07C2523/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tatalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/656—Manganese, technetium or rhenium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/02—Sulfur, selenium or tellurium; Compounds thereof
- C07C2527/057—Selenium or tellurium; Compounds thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
L'invention concerne un procédé permettant de produire une oléfine, selon lequel il est formé un flux d'alimentation de réaction qui contient au moins une paraffine, de l'oxygène et de l'eau, selon le procédé, une partie de la paraffine et de l'oxygène est convertie en oléfine dans le flux d'alimentation de réaction de manière à obtenir un gaz de processus par déshydratation oxydative au moyen d'un catalyseur, le gaz de processus contient au moins la part de paraffine et d'oxygène non convertie, l'oléfine et l'eau provenant du flux d'alimentation de réaction. Selon l'invention, il est prévu de déterminer au moins une caractéristique qui indique une activité du catalyseur ainsi que d'ajuster une quantité d'eau dans le flux d'alimentation de réaction, sur la base de ladite au moins une caractéristique déterminée. La présente invention concerne également une installation (100) correspondante.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP16206447.1A EP3339276A1 (fr) | 2016-12-22 | 2016-12-22 | Procédé et installation de production d'une oléfine |
EP16206447.1 | 2016-12-22 | ||
PCT/EP2017/084341 WO2018115418A1 (fr) | 2016-12-22 | 2017-12-22 | Procédé et installation pour produire une polyoléfine |
Publications (1)
Publication Number | Publication Date |
---|---|
CA3043162A1 true CA3043162A1 (fr) | 2018-06-28 |
Family
ID=57794071
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA3043162A Pending CA3043162A1 (fr) | 2016-12-22 | 2017-12-22 | Procede et installation pour produire une polyolefine |
Country Status (8)
Country | Link |
---|---|
US (1) | US10919821B2 (fr) |
EP (2) | EP3339276A1 (fr) |
CN (1) | CN110225900B (fr) |
AU (1) | AU2017382046A1 (fr) |
CA (1) | CA3043162A1 (fr) |
EA (1) | EA038967B1 (fr) |
WO (1) | WO2018115418A1 (fr) |
ZA (1) | ZA201904410B (fr) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP4015495A1 (fr) | 2020-12-18 | 2022-06-22 | Linde GmbH | Procédé et installation de fabrication d'un composé cible |
DE102021202495A1 (de) | 2021-03-15 | 2022-09-15 | Clariant International Ltd. | Verfahren und anlage zur herstellung einer zielverbindung |
EP4059595A1 (fr) | 2021-03-15 | 2022-09-21 | Linde GmbH | Production d'éthylène par déshydrogénation oxydative de l'éthane |
DE102021202500A1 (de) | 2021-03-15 | 2022-09-15 | Clariant International Ltd. | Verfahren und Anlage zur Herstellung einer Zielverbindung |
DE102021202505A1 (de) | 2021-03-15 | 2022-09-15 | Clariant International Ltd. | Verfahren und Anlage zur Herstellung einer Zielverbindung |
DE102021202492A1 (de) | 2021-03-15 | 2022-09-15 | Clariant International Ltd. | Verfahren und anlage zur herstellung einer zielverbindung |
EP4116283A1 (fr) | 2021-07-06 | 2023-01-11 | Linde GmbH | Procédé et installation de fabrication d'acétate de vinyle |
EP4122591A1 (fr) | 2021-07-23 | 2023-01-25 | Linde GmbH | Procédé et installation de fabrication d'un composé cible |
CN118742530A (zh) | 2021-12-08 | 2024-10-01 | 林德有限公司 | 用于生产一种或多种烃的方法和系统 |
EP4342873A1 (fr) | 2022-09-26 | 2024-03-27 | Linde GmbH | Procédé et installation de production d'éthylène et d'acide acétique, procédé et installation de production d'un composé cible à l'aide d'éthylène et d'acide acétique |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0026243D0 (en) * | 2000-10-26 | 2000-12-13 | Bp Chem Int Ltd | Process |
MX2008015540A (es) * | 2007-12-26 | 2009-06-26 | Rohm Ahd Haas Company | Un proceso integrado para preparar un acido carboxilico a partir de un alcano. |
US8519210B2 (en) * | 2009-04-02 | 2013-08-27 | Lummus Technology Inc. | Process for producing ethylene via oxidative dehydrogenation (ODH) of ethane |
CN104203401B (zh) * | 2012-03-28 | 2016-08-17 | 罗门哈斯公司 | 制造乙烯和乙酸的方法 |
EP2716622A1 (fr) | 2012-10-05 | 2014-04-09 | Linde Aktiengesellschaft | Installation de réacteur et procédé pour la déshydrogénation oxydative d'alcanes |
-
2016
- 2016-12-22 EP EP16206447.1A patent/EP3339276A1/fr not_active Withdrawn
-
2017
- 2017-12-22 EA EA201990994A patent/EA038967B1/ru unknown
- 2017-12-22 EP EP17822686.6A patent/EP3558910B1/fr active Active
- 2017-12-22 CA CA3043162A patent/CA3043162A1/fr active Pending
- 2017-12-22 US US16/472,418 patent/US10919821B2/en active Active
- 2017-12-22 AU AU2017382046A patent/AU2017382046A1/en not_active Abandoned
- 2017-12-22 WO PCT/EP2017/084341 patent/WO2018115418A1/fr unknown
- 2017-12-22 CN CN201780079406.5A patent/CN110225900B/zh active Active
-
2019
- 2019-07-04 ZA ZA2019/04410A patent/ZA201904410B/en unknown
Also Published As
Publication number | Publication date |
---|---|
EP3339276A1 (fr) | 2018-06-27 |
US10919821B2 (en) | 2021-02-16 |
US20190359544A1 (en) | 2019-11-28 |
EP3558910B1 (fr) | 2020-12-02 |
EA038967B1 (ru) | 2021-11-16 |
AU2017382046A1 (en) | 2019-05-30 |
ZA201904410B (en) | 2021-08-25 |
EA201990994A1 (ru) | 2020-01-22 |
CN110225900A (zh) | 2019-09-10 |
EP3558910A1 (fr) | 2019-10-30 |
CN110225900B (zh) | 2023-08-29 |
WO2018115418A1 (fr) | 2018-06-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request |
Effective date: 20221201 |
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EEER | Examination request |
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EEER | Examination request |
Effective date: 20221201 |